NDC 55111-613
Pramipexole dihydrochloride 1.5 mg tablet, extended release
On the label: Dr.Reddy's Laboratories Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Product details
- Generic drug
- Pramipexole: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 1.5 mg
- Approval
- ANDA ANDA203354
- On the market since
- Aug 14, 2015
- Package NDCs
55111-613-30- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?